Variant #0000291240 (NC_000021.8:g.47648479C>T, NM_003906.3:c.*6703G>A (MCM3AP))

Chromosome 21
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.47648479C>T
DNA change (hg38) g.46228565C>T
Published as LSS(NM_002340.6):c.49G>A (p.E17K)
ISCN -
DB-ID LSS_000007
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LSS NM_002340.5 ?/. - c.49G>A r.(?) p.(Glu17Lys)
MCM3AP NM_003906.3 ?/. - c.*6703G>A r.(=) p.(=)


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